-200521470 九、發明說明: 【發明所屬之技術領域】 本發明係關於在乙烯醇糸樹脂薄膜上吸附職並經配向 處理而構成的偏光膜片、以及採用該偏光膜片之偏光板及 ,液晶顯示裝置。 【先前技術】 在聚乙烯醇系樹脂薄膜上吸附碘並使配向而成的偏光 膜早已習知。此種偏光膜通常係在單面或雙面上貼合保護 膜而成為偏光板,並被用為液晶顯示裝置用組件之一。此 外,在液晶顯示裝置中,為求達成色彩重現性優越的彩色 顯示’期待達成良好的白色顯示,所以,當配置成平行偏 光㈣allel-Nico!)之際,具有無色彩色相的偏光膜廣受期 待。此種偏光膜已知有例如日本特開2〇〇2_2295〇號公報 所揭不的偏光膜。 再者,近年在桌上型電子計算機、電子時鐘、個 腦、行動電話、PDA(pers〇naIdigitalassistant)、汽車或機 重領域中’已然演變為使用液晶顯示裝置 配人^途不裳置之利用領域的擴大,便期待提昇 室㈣車内:耐久性。具體而言,當使用於 %况或者使用為機器儀表等狀況砗Φ 求能在高溫條件下、 ’更要 示裝置。所《’便要求當在高=Β::!=液晶顯 之!,光學特性劣化情況較少,即耐久:較:::: 光版及偏光板。么τ女肖 呵的偏 、、二改良南溫高濕條件下之耐久性者,已知 316317 5 200521470 有例如日本特開平2_43504號公報中所揭示的偏光膜。 【發明内容】 但疋,如上述,習知在平行偏光配置之際具有無色彩 ^相的偏光膜,潛在有在南溫條件下、冑溫冑濕條件下光 '子特性耐久性偏低的問題。 ' 叫對於常被採用作為偏光元件之吸附碘並經配向處 理而成的偏光膜之耐久性提昇方本 ,,^人丨玍杈幵方法,已知有增加偏光膜中 朋酸含量等方法。當將此種耐久性提昇方法使 c°具有無色彩色相之偏光膜時,例如增加蛾化 雖??昇耐久性,卻將發生偏光膜的色相變 I…^而疋王現偏向黃色色相的問題。此外,杏辦 久性將提昇,但是相2 條件下的光學特性之耐 久性卻發生降低的問題。回/皿條件下的光學特性之耐 種在==爾決上述問題,其目的在於提供- 濕=ί.=Γ現無色彩色相,而且在高溫高 1木1干卜及回,農條件下的光學 ^ 此外,另一目的/担 、十鬲的偏光膜。 勺在^供一種採用該偏光 的偏光板以及液晶顯示裝置。 、/、有问耐久性 (解決課題之手段) :案發明者等為解決上述課題,經 現精由從含有石朋酸與特定範圍之 鐵研、、·。果,發 薄膜製得之偏光膜、以及由1所:周 ^乙烯醇系樹脂 裝置可達成上述㈣,遂完成本發日;^爲光=反與液晶顯示 &月亦即本發明係關於·· 3] 63 Π 6 200521470 〇)一種偏錢,係由吸附石典並、經配向(〇iie處刚)處理 的聚乙稀醇系樹脂所構成之偏光膜,其中以含有蝴酸與 200至10,〇〇〇ppm氯離子為其特徵者; ⑺如(1)之偏光版’其中,偏光膜中的硼酸含量為$ 至40重量%者; (3)如⑴或(2)之偏光膜之製法,係對聚乙烯醇系樹脂 薄膜,依任意順序施行碘處理(染色處理)、延伸處理 '以 及石朋酸處理,獲得含有硼酸與硬的聚乙稀醇系樹脂薄膜, 再以含有氯化合物的水溶液施行處理為1 W如⑴或(2)之偏光膜之製法,係對聚乙烯醇系樹脂 薄膜施行碘處理(染色處理)之後,再依序施行延伸處理、 硼酸處理、含有氣化物之水溶液處理為其特徵者; (5) —種偏光板,係在(1)或(2)之偏光膜之單面或雙面 上貼合保護膜而成者; (6) 如(5)之偏光板,其中,保護膜係醋酸酯系樹脂薄膜 者; (7) 如(5)之偏光板,其中,保|隻膜係聚烯烴系樹脂薄膜 者; (8) —種液晶顯示裝置,係具備(5)至(7)中任一項之偏 光板而成者。 (發明之效果) 依照本發明,可達成無色彩色相,且在高溫條件下與 高溫高濕條件下的光學特性之耐久性優越之偏光膜及偏光 板。此外’可達成良好的白色顯示並且在高溫條件下及高 316317 7 200521470 溫高濕條件下的耐久性高之液晶顯示裝 晶顯示裝置的利用領域。 °更加擴大液 【實施方式】 以下,針對本發明的較佳實施形態進行說明。 本發明中所使用的偏光膜,係在聚乙歸醇李樹 亡:附石典並經配向處理而成者,例如在對聚 曰樹: ;:以,嶋理之後或同時,施行延伸處理:、= ^里、以及浸潰於含氯化物之水溶液中的補色處理而料 ⑪乙系樹脂薄膜的原料’通常係使用聚乙稀醇或 :乙㈣質體,其聚合度係1000至1〇,〇〇〇左右之成-200521470 IX. Description of the invention: [Technical field to which the invention belongs] The present invention relates to a polarizing film constituted by adsorption and alignment treatment on a vinyl alcohol resin film, and a polarizing plate and a liquid crystal using the polarizing film. Display device. [Prior Art] A polarizing film formed by adsorbing and aligning iodine on a polyvinyl alcohol-based resin film has long been known. Such a polarizing film is usually a protective film laminated on one or both sides to become a polarizing plate, and is used as one of components for a liquid crystal display device. In addition, in the liquid crystal display device, in order to achieve a color display with excellent color reproducibility, 'good white display is expected, so when it is configured as parallel polarized light (allel-Nico!), A polarizing film having a colorless color phase is widely used. Expect. Such a polarizing film is known, for example, a polarizing film disclosed in Japanese Patent Application Laid-Open No. 2000-2295. In addition, in recent years, in the field of desktop electronic computers, electronic clocks, personal computers, mobile phones, PDAs (Persian Digital Assistant), automobiles, and machine weights, it has evolved to use liquid crystal display devices for human use. With the expansion of the field, we look forward to improving the durability of the car: durability. Specifically, when it is used under the condition of “%” or “machine and instrument”, it is necessary to be able to indicate the device under high temperature conditions. Therefore, "’ requires that when the high = Β ::! = LCD display! , Less degradation of optical characteristics, that is, durable ::::: light plate and polarizer. The female polarizer, π, and the polarizer, which improve the durability under high temperature and humidity conditions in the south, are known. 316317 5 200521470 For example, there is a polarizing film disclosed in Japanese Patent Application Laid-Open No. 2_43504. [Summary of the Invention] However, as mentioned above, it is known to have a colorless phase polarizing film in a parallel polarized configuration, potentially having a low photon characteristic durability under the conditions of south temperature and high temperature and humidity. problem. The method for improving the durability of a polarizing film that is often used as a polarizing element to absorb iodine and undergoes alignment treatment is known as a method of increasing the acid content in a polarizing film. When this durability improvement method is used to make c ° a polarizing film with a colorless color phase, for example, mothization is increased. ? If the durability is improved, the hue change of the polarizing film will occur I ... ^, and the problem that the king is now biased to the yellow hue. In addition, the durability of apricots will be improved, but the durability of the optical characteristics under phase 2 conditions will be reduced. The resistance to optical characteristics under the conditions of back / dish is determined by the above problems, and its purpose is to provide-wet = ί. = Γ colorless color phase, and high temperature 1 wood 1 dry and back, under agricultural conditions Optical ^ In addition, another purpose / load, ten 鬲 polarizing film. The present invention provides a polarizing plate using the polarized light and a liquid crystal display device. Inquiry durability (means for solving the problem): In order to solve the above-mentioned problems, the inventors of the case have found out that the iron oxide containing a pectic acid and a specific range has been used. As a result, a polarizing film made of a hair film, and a vinyl alcohol resin device can achieve the above-mentioned requirements, and then the present day is completed; ^ is light = reflective and liquid crystal display & month, that is, the present invention is about ·· 3] 63 Π 6 200521470 〇) A kind of partial money, which is a polarizing film made of polyethylene resin based on adsorption stone code and treated with aligning (just before), which contains butterfly acid and 200 Characterized by chloride ion to 10,000 ppm; (e.g., the polarized version of (1), where the boric acid content in the polarizing film is $ to 40% by weight; (3) polarized light such as ⑴ or (2) The production method of the film is to perform an iodine treatment (dyeing treatment), an elongation treatment, and a lithonic acid treatment on a polyvinyl alcohol resin film in any order to obtain a polyvinyl alcohol resin film containing boric acid and hard, and then An aqueous solution of a chlorine compound is treated as a 1 W polarizing film such as Rhenium or (2). After applying an iodine treatment (dyeing treatment) to a polyvinyl alcohol resin film, it is sequentially subjected to an extension treatment, a boric acid treatment, and a gas containing solution. Aqueous solution of chemical compounds is characterized by it; (5) — species bias Plate, which is obtained by laminating a protective film on one or both sides of the polarizing film of (1) or (2); (6) The polarizing plate of (5), wherein the protective film is an acetate resin film (7) A polarizing plate such as (5), in which the film is only a polyolefin resin film; (8) A liquid crystal display device having any one of (5) to (7) Made of polarizing plate. (Effects of the Invention) According to the present invention, a polarizing film and a polarizing plate capable of achieving a colorless color phase and having excellent durability of optical characteristics under high-temperature conditions and under high-temperature and high-humidity conditions can be achieved. In addition, it can achieve a good white display and a high-temperature and high-temperature durability 316317 7 200521470 high-temperature and high-humidity liquid crystal display device. ° More enlarged liquid [Embodiment] Hereinafter, a preferred embodiment of the present invention will be described. The polarizing film used in the present invention is made of polyethylene terephthalate and plum tree: attached with a stone code and subjected to an orientation treatment, for example, after the polycrystalline tree:;: after or at the same time, an extension treatment is performed :, = ^ Li, and color-compensating immersion in a chloride-containing aqueous solution, the raw material of the B-series resin film 'usually uses polyvinyl alcohol or: acetam plastid, the degree of polymerization is 1000 to 1 〇, 〇〇〇
Ba 图乙坤知乐樹脂薄膜乃藉由脾i曰 =乙稀醇系樹脂進行製膜而製得者。製膜可採用週= 左T:。聚乙_系樹脂薄膜之厚度通常為5—至i5 — 將聚乙烯醇系樹脂薄膜膨潤之後,以碘施行染色處 、、夜等ΓΓΓ染色處理係例如在含有蛾與石典化卸的水溶 /寺之中’甚至更含有石朋酸的染色溶液中,浸潰上述〒乙 P系樹脂薄膜而施行。當採用水溶液時,該水溶液中的 0、、:典化鉀之使用量係相對於水⑽重量份,石典為0 0】至 A 50 C左右。浸潰時間係】0至300秒左右之 Π6317 ‘200521470 使聚乙烯醇系樹脂 範圍。藉由此種以碘施行的染色處理 薄膜吸附ί典。 其次,對已吸附蛾的聚乙稀醇系樹㈣膜,施行既定 伸的延伸處理。延伸處理係使聚乙烯醇系樹 潰在酸水溶液中實施。髮水溶液㈣酸使用 相對於水1GG重量份酸為3.〇重量份左右“朋酸水 溶液的溫度係例如30 i 6Gt:左右。延伸方法可採行使用 熱輥施行的方法,亦可在圓周速度不同的二輥之間施行單 軸延伸的方法。延伸倍率通常為4 〇至7 〇倍左右。 ^硼酸處理係將已施行上述染色處理、延伸處理的聚乙 烯醇系樹脂薄膜浸潰在硼酸水溶液中而實施。硼酸處理的 硼酸水溶液係採用相對於水1〇〇重量份,溶解硼酸3 〇至 7·〇重里h ’最好為4·〇至6·0重量份而成者。酸水溶液 的溫度係例如在4(TC以上,最好為50至85^。浸潰時間 在上述溫度中係為例如10至6〇〇秒,最好為3〇至3〇〇秒。 如上所述,藉由在硼酸水溶液中施行的延伸處理以及 :酸處理,使本發明的偏光膜含有硼酸。偏光膜的硼酸含 量係5至40重量%。i好為15至25重量%。藉由分別調 整延伸處理及硼酸處理中的硼酸濃度、浸潰時間、溶液溫 度’便可調整所獲得偏光膜的硼酸含量。 補色處理係將已施行上述染色處理、延伸處理、硼酸 處理的聚乙烯醇系樹脂薄膜,浸潰於含氯化物的水溶液(以 下稱氯化物水〉谷液」)中而實施。氣化合物水溶液係採用 相對於水1 00重量份,溶解氯化物〇·丨至1 〇重量份,最好 316317 9 200521470 為1.0至5.G重量份者。氣化合物水溶液的溫度係例如如 至70t。浸潰時間係在上述溫度中為例如ι〇至秒。 藉由施行補色處理,有使蛾離子狀態呈安定化而不易發生 色變化的效果。 調製氯化物水溶液時所使用的氯化物,可舉例如:氯化 '鉀、氯化鈉、氯化鋰等鹼金屬氯化物,或如:氯化鈹、氯化 鎂、氯化辦等驗土族金屬氯化物,或如:氣化銘、氯化辞等 金屬氯化物等。 藉由加订補色處理,使偏光膜含有氣離子。偏光膜的 氯離子含量係200幻〇,_ppm,最好為3〇〇至遲卯… 依此便可㈣同時含有硼酸與氯離子2〇〇至! 偏絲。補色處理後施行水洗、乾燥處理。乾燥處理中的 乾無溫度係4〇i5(rC左右,乾燥時間係60秒左右。 :光財的顯濃度,係將㈣得之偏錢在純水中 加熱使完全溶解’然後添加_(P—一)指示劑, 隹子:f水’合液進仃中和滴定而求得。氣離子濃度係利· 用_子層析法(達歐納克斯公司(音譯)製Μ_32〇)求得。 ::所獲传本發明的偏光膜,係藉由含有硼酸及—定 ^柯孔t 1 $成在南溫條件下與高溫高濕條件下的高耐 ':亚且在平行偏光配置之際達成無色彩狀態。 本發明並不受限於上述實施形態 理設定在心施行” / ^形悲中,雖然將延伸處 施行染色處理之前:或:理之後才實施,但是亦可在以峨 2在以蛾施行染色處理中實施。此外, ]〇 316317 200521470 2酸處理中亦可施行延伸處理。另夕卜例如亦可為在大 孔把订延伸的乾式延伸。當在以硬施行染色處理中 延二處理^或在顯處理中施行延伸處理,或施行乾式延 伸日才’所獲得偏光膜的酸含量,宜調整為僅利用顯 理時之5至40重量%範圍内。 护/迟之L伸處理若與以蛾施行染色處理或硼酸處理同 、進行或轭行乾式延伸時,亦可將硼酸處理的硼酸水溶 液=顯濃度設定為較上述實施形態中之範圍更高,亦可 將α ’貝日守間设定為較上述實施形態中的範圍更長。 σ八再者例如亦可將延伸處理分數次實施,硼酸處理亦 可刀數_人貝施。此外,例如在以碘施行染色處理時的碘染 ,溶可含有硼酸。在該等情況中,各處理的硼酸濃 π /貝日^間、>谷液溫度並未限定於上述實施形態的範圍 内,可將偏光膜中的硼酸含量適當調整為5至4〇重量%。 '本發明的偏光板係在依上述所獲得本發明偏光膜的單 面或雙面上貼合保護膜而成者。纟中,保護膜乃為提昇偏 ,膜的耐水性與處置性等目的而附加者,在其形成方面可 ^用適當的透明物質。尤其以使用透明性、機械強度、熱 安水分阻絕性等均優越的塑膠等為佳。其中之例如 由:δ曰;^树月曰、醋酸酯系樹脂、聚醚砜系樹脂、聚碳酸酯 系樹脂、聚醯胺系樹脂、聚醯胺系樹脂、聚烯烴系樹脂、 及1烯酸系樹脂等熱可塑性樹脂;丙稀酸系、胺醋系、丙 稀酸胺S旨系、環氧系及㈣等熱硬化性樹脂;或紫外線硬 化性樹脂等所獲得的薄膜。該等之中,聚婦烴系樹脂可舉 3J6317 11 200521470 例如具有如甲萡烯等非晶性聚烯烴 :烯系單體之環狀聚烯煙聚合單位的樹脂。較 如三乙醯基纖维辛ίΤΑη笙 的保' 4 Μ 土、戴、,择京(1AC)寺。此外,保護層 明保護膜在不損及本發明目的 用勺透 王f十4工e „ 士 月』徒下亦可施行硬塗處 或杬反射處理、以及防止影像殘留或擴散 目的之處理等等。 寻為 ^日^偏光膜與保護膜之黏著處理並無特別限制, 例如可使用由聚乙烯醇系聚合物 酸、石^,卜“ — 吓稱戚之黏者劑、或由硼 =—⑯、—*氰、草酸等乙烯醇系聚合物之 ?容***聯劑所構成黏著劑;透明性佳的環氧系樹脂、聚 酯系樹脂、醋酸乙稀醋等溶劑型黏著劑;或丙稀酸系樹脂: 胺酯樹脂等依聚合反應而硬化的黏著性樹脂等等而實施曰。 ,本發明的偏光板亦可使用為積層於其他光學材料之光 學層上的光學組件。例如將反射板、半穿透反射板、相位 差板(包括1/2波長板、1/4波長板等λ板在内)、視角補償 膜或輝度提昇膜等,在液晶顯示裳置等形成時所採用的適 當光學材料,積層丨層或2層以上。具體例有在本發明的 偏光膜上更積層反射板或半穿透反射板所構成的反射型偏 光板或半穿透反射型偏光板,同樣的在本發明的偏光板 上,更積層相位差板而成的橢圓偏光板或圓偏光板,或在 本發明的偏光板上積層視角補償膜的偏光板,或在本發明 的偏光板上更積層輝度提昇膜的偏光板等。 再者,採用本發明偏光板的各種光學組件,可適用於 液晶顯示裝置等各種裝置的形成。例如,可使用於將本發 η 316317 200521470 明偏光板配置於液晶單元 穿透型、或穿透·反射雙用型等液:::=反射型、 下,形成液晶顯示裝置的液晶單元係可' 者中。此情况 使用薄膜電晶體型所代表的主動矩陣驅動型列如可 <列型、超扭轉向㈣為代表的單純矩 ^ ^向 式的液晶單元。 力尘寺寺適當型 η 再者,當在液晶單元二側設置 該等可為相同亦可Λ不π Α先予紐件時, 邳ij丌了為不同。此外,當 際’亦可在例如稜鏡陣列薄片、透鏡陣列薄片、之 背光板等適當組件之適當位置處配 先:放板、 當將偏光板當作液晶顯示裝置組件使用時 層。此黏著層之形成,可採;早適;的黏著 ^ . 週田的黏者性物質或黏著劑, 二舉例如以丙烯酸系⑽ σ 、小㈣、聚醯胺、聚醚、氟系、橡膠车耸、南 當聚合物為基底聚合物者。 / 、 本發明的偏光板係可使用於如扭轉向列方式⑽: :ed Nemaiic)、超扭轉向列方式(stn)、薄膜電晶體方 Μ顯示^直配向方式(VA)、平面扭轉模式(IPS)等全部 以下,舉實施例更具體說明本發明。 (實施例) 實施例1 將聚乙歸醇系樹脂薄膜(厚度75μ1Ώ)(可樂麗股份有限 316317 13 200521470 公司(音譯)製VF-XS),在3〇t水中膨潤5分鐘之後,再於 机的染色液(相對於水1 00重量份,含有蛾0.05重量份、 二鉀:二里份)中浸潰5分鐘,俾進行以蛾施行的染色 :二二在5〇 C的3重量。相酸水溶液中延伸5.5倍而 *」_:传延伸薄月莫。經延伸處理後,將延伸薄膜在50t的5重 ,·量%賴水溶液中浸潰2分鐘,削4,再於3(rc的1%氣 ㈣水溶液中浸潰丨分鐘,經水洗後在机空氣中 :光t發明广偏光膜。所獲得偏光膜的厚度為25μηι。 偏先版中的石朋酸濃度係利用中和滴定法求得,氣離 dx_32〇^- 付。偏光膜的硼酸含量係22 U00Ppm〇 里係22·。重!%,氯離子含量係 声丁 膜之雙面上,利用聚乙婦醇系黏著劑叠 7曰Ο—富士照片軟夥f T8〇UZ)之後,於 色相^5〇Γ1^得偏.此偏光板係平行偏光中的 明委。八:广 =0·64(色相,b*係表示由國際- r委貝會(CE)所決定的色座標)之無色彩者。 貫施例2 將命乙稀醇系樹脂薄膜( 重=靴的染色液(相對於水_重量份心^^ =色=鉀I?量份)中浸潰5分鐘,俾進行 U倍而獲得延伸^…的3重量%石朋酸水溶液令延伸 n専概。經延伸處理後,將延伸薄膜在5〇 3]6317 14 200521470 。(:的5%硼酸水溶液中浸潰2分鐘,然後,再於3〇。〇的 氣化鈉水溶液中浸潰丨分鐘,經水洗後,在刊它空氣中乾 燥而獲彳寸本發明的偏光膜。偏光膜的硼酸含量係3重量 % ’氣離子含量係l,3〇〇ppm。 在所獲得偏光膜之雙面上,利用聚乙稀醇系黏著劑疊 層TAC薄膜(富士照片軟膠製T8〇uz)之後,於7〇。〇乾燥1 分鐘而獲得偏光板。此偏光板係平行偏光中的色相 a*=-1.18、色相b*=0.62之無色彩者。 實施例3 •將聚乙烯醇系樹脂薄膜(可樂麗股份有限公司(音譯) 製W〇CS),在3〇°C水中膨潤5分鐘之後,再將聚乙烯醇 /專膜於30 C的染色液(相對於水1〇〇重量份,含有碘〇 重量份、碘化鉀〇1重量份)中浸潰5分鐘,俾進行以碘施 行的木色處理,其次在5〇。〇的3%硼酸水溶液中延伸5.5 =而獲得延伸薄膜。經延伸處理後,將延伸薄膜在5〇。〇的 5/〇硼馱水洛液中浸潰2分鐘,然後,再於如。c的〇·〕%氯 化鉀水〉谷液中浸潰1分鐘,經水洗後,在4CTC空氣中乾燥 。而獲得本發明的偏光膜。偏光膜的硼酸含量係22·5重量 A ’氮離子含量係3 1 Oppm。 在所獲得偏光膜之雙面上,利用聚乙烯醇系黏著劑疊 層丁AC薄膜(富士照片軟膠製T8〇uz)之後,於7〇。〇乾燥$ 1知而獲得偏光板。此偏光板係平行偏光中的色相 a〜〇·87、色相b* = 0 59之無色彩者。 貫施例4 316317 15 200521470 ,將聚乙稀醇系樹脂薄膜(可樂麗股份有限公司(音譯) Γ — XS) ’在㈣水中膨潤5分鐘之後,再將聚乙稀醇 =於啊的染色液(相對於水1〇〇重量份,含有蛾〇〇5 /里伤、蛾化钾(U重量份)中浸潰5分鐘,俾進行以蛾施 订的染色處理’其次在5Q。㈢3%餐水溶液中延伸η 倍而獲得延伸薄膜。經延伸處理後,將延㈣膜在贼的 5。/。石朋酸水溶液中浸潰2分鐘,然後,再於机的π。氯化 鉀水溶液中浸潰1分鐘,經水洗後,在啊空氣中乾燥而 獲得本發明的偏光膜。偏光膜的硼酸含量係2ι·5重量%, 氣離子含量係5,0〇〇ppm。 里〇’ 在所獲得偏光膜之雙面上,利用聚乙稀醇系黏著劑疊 層TAC薄膜(富士照片軟膠製T8〇uz)之後,於7〇它乾燥$ 分鐘而獲得偏光板。此偏光板係平行偏光中的^相 a*Ul、色相b*=CK49之無色彩者。 比較例1 將聚乙烯醇(厚度75μηι)(克拉雷股份有限公司(音譯) 製VF-XS)。,在3〇°C水中膨潤5分鐘之後,再將聚乙稀醇 4膜於35C的染色液(相對於水1〇〇重量份,含有碘〇 μ 重量份、碘化鉀0.1重量份)中浸潰5分鐘,俾進行以碘施 仃的染色處理,其次在50°C的2%硼酸水溶液中延伸47 倍而獲得延伸薄膜。經延伸處理後,將延伸薄膜在乃七的 水中洗淨2分鐘,再於4〇°C空氣中乾燥而獲得比較用的偏 光膜。此偏光膜的硼酸含量係】6·5重量%,氣離子含量 30ppm 。 5 里乐 316317 16 *200521470 侧蔓得偏光膜之雙面上,利用聚乙烯醇系黏著劑最 層TAC薄膜(富士照片軟膠製T80UZ)之後,於6〇。〇乾燥5 分鐘而獲得偏光板。此偏光板係平行偏光中的色相 a*=-0.87、色相b* = 0.68之無色彩者。 如同將實施例1至實施例4以及比較例丨中所獲得本 發明之偏光板以及比較用的偏光板作為普通液晶顯示襄置 組件使用的情況,貼合於玻璃基板與液晶單元(LCD),在 咼溫條件(85 C )及咼溫高濕條件(6〇°C X 90%RH)的環境條 件下施行试驗’結果如表1所示。 表1 性能試驗 85〇Cx 1000h ~6〇°Cx 90%RHTT〇〇〇h 貼合於LCD上 的結果 偏光度變化 色變化 (△(a*.b*)) 偏光度變化 色變化 (△(a*.b*)) 實施例1 +0.3 1.9 -11.9 0.8 無顯示問題 貫施例2 +0.5 2.1 -12.4 0.9 無j員示問題 員施例3 +0.3 1.8 -15.7 2.8 無顯示問題 夏施例4 +03 2.0 -14.4 2.2 無顯示問題 比較例1 +1.8 10.4 -26.5 4.1 顯示較淡、 無法看到 表1所示係在高溫條件(85。〇及高溫高濕條件(6(TCx 90%)下,分別施行放置looo小時之試驗時的「偏光度變 化」、「色變化(△ a*.b*)」、及「貼合於LCD上的結果」。其 中,所謂「偏光度變化」係指試驗前與試驗後的偏光度差, +係指試驗後的偏光度較試驗前的偏光度上升,”」,係指 試驗後的偏光度較試驗前的偏光度減少。此外,「色變化(△ a*.b*)」係數學式+ 。△”、Δί3* 係分 316317 -200521470 別指試驗前與試驗後的平行偏光中之色相a*變化量,色相 b*變化量。亦即△ (a*.b*)係指試驗前與試驗後的偏光板色 相雙化。所s胃「貼合於LCD的結果」係指利用目視評估各 試驗後的液晶顯示狀態之結果。 如表1所示,本發明的偏光板在高溫條件(85。〇及高 溫高濕條件(6Gt:X 9G%)下,長時間(_Gh)放置後的偏光 度變化,較少於比較例丨所示偏光板,且 此外,相對於比較例丨所示偏光板的數值,二明為::板 的色變化uw))數值較小。此顯示本發明的偏光^ 乎未引發變色,亦即在試驗後仍保持著無色彩的色相。另 外本I明的液晶顯示狀態亦無任何問題發生。 316317 18Ba Tu Yikun Zhile resin film is made by spleen i = vinyl alcohol resin. Film formation can be done with week = left T :. The thickness of polyethylene resin film is usually 5 to i5. After the polyvinyl alcohol resin film is swollen, the dyeing process is performed with iodine, cyan, etc. ΓΓΓ dyeing treatment system, for example, in water-soluble Sizhong 'was even impregnated with the above-mentioned Phenyl P-based resin film in a dyeing solution containing pitonic acid. When an aqueous solution is used, the amount of potassium phosphate in the aqueous solution used is about 0 to about 50 C, based on parts by weight of water hydration. The impregnation time is about 0 to 300 seconds. Π6317 ‘200521470 makes the polyvinyl alcohol resin range. Films adsorbed by this dyeing treatment with iodine. Secondly, the polyvinyl alcohol-based tree shrew membrane to which the moth has been adsorbed is subjected to a predetermined extension treatment. The stretching treatment is performed by subjecting the polyvinyl alcohol-based tree to an acidic aqueous solution. The temperature of the aqueous solution of gallic acid is about 3.0 parts by weight with respect to 1GG parts by weight of water. The temperature of the aqueous solution of the acid is, for example, 30 i 6Gt: about. The extension method can be performed by using a hot roller or at a peripheral speed. Uniaxial stretching is performed between different two rolls. The stretching ratio is usually about 40 to 70 times. ^ Boric acid treatment is a process in which the polyvinyl alcohol resin film that has been subjected to the above-mentioned dyeing treatment and stretching treatment is immersed in an aqueous solution of boric acid. The boric acid-treated aqueous solution of boric acid is prepared by dissolving boric acid at 30 to 7.0 weight% with respect to 100 parts by weight of water, preferably at 4.0 to 6.0 weight parts. The temperature is, for example, 40 ° C. or higher, preferably 50 to 85 ° C. The impregnation time is, for example, 10 to 600 seconds, and preferably 30 to 300 seconds at the above temperature. As described above, borrow The polarizing film of the present invention contains boric acid by the stretching treatment performed in the boric acid aqueous solution and the acid treatment. The boric acid content of the polarizing film is 5 to 40% by weight. The i is preferably 15 to 25% by weight. The extension processing is adjusted separately. And boric acid concentration in boric acid treatment Degree, impregnation time, and solution temperature 'can adjust the boric acid content of the obtained polarizing film. The color correction process is a polyvinyl alcohol-based resin film that has been subjected to the above-mentioned dyeing treatment, stretching treatment, and boric acid treatment, and is immersed in a chloride-containing resin film. It is implemented in an aqueous solution (hereinafter referred to as "chloride water> valley"). An aqueous solution of a gaseous compound is prepared by dissolving chloride in an amount of 0.1 to 10 parts by weight with respect to 100 parts by weight of water, preferably 316317 9 200521470 at 1.0 to 5 .G parts by weight. The temperature of the gas compound aqueous solution is, for example, up to 70t. The impregnation time is, for example, ι0 to seconds at the above-mentioned temperature. By performing a color supplement treatment, the moth ion state is stabilized and the color is not easily generated. The effect of the change. The chloride used in the preparation of the chloride aqueous solution may include, for example, alkali metal chlorides such as potassium chloride, sodium chloride, and lithium chloride, or beryllium chloride, magnesium chloride, and chloride office. Check the metal chlorides of the Tu group, or metal chlorides such as gasification and chlorination. By adding color correction, the polarizing film contains gas ions. The chloride ion content of the polarizing film is 200 p. It is better to be 300 to late… This will allow you to contain boric acid and chloride ions at the same time! Partial yarns. After color correction treatment, water washing and drying treatment will be performed. The dry temperature in the drying treatment is 40i5 ( About rC, the drying time is about 60 seconds.: The significant concentration of Guangcai, is the partial money that is won in the pure water is heated to completely dissolve 'then add _ (P- 一) indicator, Gardenia: f water' The mixture is obtained by neutralization and titration. The gas ion concentration is determined by using chromatographic chromatography (Daonax Corporation (M_32)). :: The obtained polarizing film of the present invention It is based on containing boric acid and -determining Ke Kong t 1 $ to achieve high resistance under the conditions of South temperature and high temperature and high humidity conditions: and achieve a colorless state in the configuration of parallel polarized light. The present invention is not limited to the above-mentioned embodiment. It is set in the heart application. Although it is performed before the extension is dyed: or: after the treatment, the dyeing treatment can also be performed on the moth with E2. In addition,] 0316317 200521470 2 extension treatment can also be performed in the acid treatment. In addition, for example, it can be a dry extension of a large hole in the extension. When the dyeing treatment is performed in a hard way ^ or in the display The acid content of the polarizing film obtained by the extension treatment during the treatment, or by the dry extension genius, should be adjusted to be within the range of 5 to 40% by weight when using the sensation. When dyeing treatment or boric acid treatment is performed in the same or performed in the dry extension, the boric acid-treated boric acid aqueous solution = significant concentration can also be set to a higher range than in the above embodiment, and α'Beri Mori can also be set to The range is longer than that in the above embodiment. Σ Eight or more, for example, the extension treatment can be performed in several times, and the boric acid treatment can also be performed with the number of knifes_person besch. In addition, for example, iodine dyeing when the dyeing treatment is performed with iodine. The solvent may contain boric acid. In these cases, the boric acid concentration of each treatment is π / Beijing, and the valley temperature is not limited to the range of the above embodiment, and the boric acid content in the polarizing film may be appropriately adjusted to 5 to 40% by weight. 'The polarizing plate of the present invention is obtained by laminating a protective film on one or both sides of the polarizing film of the present invention obtained as described above. In the middle, the protective film is for improving the polarization. Appropriate transparent materials can be used for the purpose of water resistance and disposal. In particular, it is preferable to use plastics that are excellent in transparency, mechanical strength, heat and moisture resistance, etc. Among them, : δ said; ^ tree month said, acetate resin, polyethersulfone resin, polycarbonate resin, polyamide resin, polyamide resin, polyolefin resin, and 1 enoic resin, etc. Thermoplastic resins; thermosetting resins such as acrylic, acetic acid, and acrylic amine S, epoxy and fluorene; or films obtained from ultraviolet curable resins. Examples of hydrocarbon resins include 3J6317 11 200521470 Amorphous polyolefin such as olefin: Resin of cyclic polyene smoke polymerized unit of olefinic monomer. It is more like triethylfluorinated fiber Xin ΤΑη Sheng's Bao '4 MU soil, wear, and select Beijing (1AC) temple In addition, the protective layer and the protective film can also be used for hard coating or reflection treatment, as well as for preventing the image retention or diffusion purpose, without undermining the purpose of the present invention. and many more. The adhesive treatment of the polarizing film and the protective film is not particularly limited. For example, a polyvinyl alcohol polymer acid, a stone, or a boron agent can be used, or a boron agent can be used. --- * Cyanine, oxalic acid and other vinyl alcohol-based polymers? Capacitive cross-linking agent composed of adhesives; transparent epoxy resins, polyester resins, vinyl acetate and other solvent-based adhesives; or acrylic Acid resins: Adhesive resins such as urethane resins that are hardened by polymerization, etc. The polarizing plate of the present invention can also be used as an optical component laminated on the optical layer of other optical materials. For example, a reflective plate , Transflective reflectors, retardation plates (including λ plates such as 1 / 2-wavelength plates and 1 / 4-wavelength plates), viewing angle compensation films or brightness enhancement films, etc. Appropriate optical material, laminated or more than two layers. Specific examples include a reflective polarizing plate or a transflective polarizing plate composed of a reflective plate or a transflective reflective plate laminated on the polarizing film of the present invention. On the polarizing plate of the present invention, the phase difference is further stacked. An elliptical polarizer or a circular polarizer, or a polarizer with a viewing angle compensation film laminated on the polarizer of the present invention, or a polarizer with a brightness enhancement film further laminated on the polarizer of the present invention. The various optical components of the polarizing plate of the present invention can be applied to the formation of various devices such as a liquid crystal display device. For example, the polarizing plate of the present invention can be used to dispose the liquid crystal cell transmissive type, or dual-use transmission and reflection Type liquid ::: = reflective type, the liquid crystal cell forming the liquid crystal display device may be used. In this case, the active matrix driving type represented by the thin film transistor type such as can be < row type, super twist direction ㈣ is a representative liquid crystal cell of the simple moment ^ ^ direction. Lichensi Temple appropriate type η Furthermore, when these are set on the two sides of the liquid crystal cell, they can be the same or Λ not π Α pre-buttons, 邳 ij It ’s different. In addition, when it ’s time, it can also be placed at the appropriate position of the appropriate components such as the 稜鏡 array sheet, lens array sheet, backlight panel, etc .: put the board, when the polarizing plate is used as a liquid crystal display device assembly Time The formation of this adhesive layer can be adopted; early adaptation; adhesion ^. Zhou Tian's adhesive substances or adhesives, for example, acrylic acrylic ⑽ σ, berberine, polyamine, polyether, fluorine 、 Rubber tower, Nandang polymer is the base polymer. / 、 The polarizing plate system of the present invention can be used in, for example, twisted nematic mode:: ed Nemaiic), super twisted nematic mode (stn), thin film transistor The square M shows the following: the direct alignment method (VA), the plane twist mode (IPS), and the like, and the present invention will be described in more detail by way of examples. (Example) Example 1 A polyethylene glycol resin film (thickness: 75 μ1 mm) ( Kuraray Co., Ltd. 316317 13 200521470 company (VF-XS), after swelling in 30t water for 5 minutes, and then the machine's dyeing solution (100 parts by weight of water, 0.05 parts by weight of moth, two potassium : Erli) for 5 minutes, the pupae were stained with moths: Erji at 3 weights at 50 ° C. The phase acid solution is stretched 5.5 times and * "_: It is extended thin mo. After the stretching treatment, the stretched film was immersed in a 50-ton, 5 wt.% Aqueous solution of Lai for 2 minutes, cut for 4 minutes, and then immersed in a 3% rc aqueous solution of 1% airborne water for 1 minute. In the air: the wide polarizing film is invented by light. The thickness of the obtained polarizing film is 25 μηι. The concentration of lithonic acid in the first edition is obtained by neutralization titration, and the gas ionization dx_32〇 ^-付. The boric acid content of the polarizing film 22 U00Ppm0, 22. Weight!%, Chloride ion content is on both sides of the butyl film, using a polyethenol-based adhesive to stack it (7-Fuji Photo Soft (f T80UZ)), then The hue ^ 5〇Γ1 ^ is polarized. This polarizing plate is a bright member in parallel polarized light. Eight: Guang = 0.64 (hue, b * is the colorless one determined by the International-R Committee (CE)). Throughout Example 2 Methoxyl-based resin film (weight = staining solution of boots (relative to water_parts by weight ^^ = color = potassium I? Parts) was impregnated for 5 minutes, and then U-folded to obtain The 3% by weight aqueous solution of lithopenic acid is used to extend the extension n. After the extension treatment, the extended film is immersed in 50% 6317 14 200521470. (: 5% boric acid aqueous solution for 2 minutes, and then, It was immersed in a 30.0% aqueous solution of sodium gas for 1 minute, washed with water, and dried in air to obtain a polarizing film of the present invention. The boric acid content of the polarizing film is 3% by weight. 1,300 ppm. On both sides of the obtained polarizing film, a TAC film (T8ouz made by Fuji Photo Soft) was laminated with a polyvinyl-based adhesive, and then dried at 70% for 1 minute. A polarizing plate was obtained. The polarizing plate was a colorless one with hue a * =-1.18 and hue b * = 0.62 in parallel polarized light. Example 3 • Polyvinyl alcohol resin film (made by Kuraray Co., Ltd.) (WOCS), after swelling in water at 30 ° C for 5 minutes, then the polyvinyl alcohol / special film was stained at 30 ° C (relative to water 1.0). Part by weight, containing iodine (0 parts by weight, potassium iodide (1 part by weight)), immersed for 5 minutes, and then treated with wood color with iodine, followed by 5.5 = 3% boric acid aqueous solution of 50.0 to obtain an extended film After the stretching treatment, the stretched film was immersed in a 5/0 solution of boron hydrazine for 5 minutes, and then immersed in a water solution such as 〇 ·]% potassium chloride water> c. After being washed for 1 minute, it was washed with water and dried in 4CTC air. The polarizing film of the present invention was obtained. The boric acid content of the polarizing film was 22.5 weight A and the nitrogen ion content was 3 1 Oppm. On both sides of the obtained polarizing film On the other hand, a polyvinyl alcohol-based adhesive was used to laminate a butadiene AC film (T8ouz made by Fuji Photo Soft), and then dried at 70% to obtain a polarizing plate. This polarizing plate is a hue a in parallel polarized light ~ 〇 · 87, the hue b * = 0 59 is colorless. In accordance with Example 4 316317 15 200521470, the polyethylene resin film (Kuraray Co., Ltd. (transliteration) Γ — XS) 'swells in the water After 5 minutes, the dyeing solution of polyvinyl alcohol = 100% (100 parts by weight with respect to water) After being immersed for 5 minutes in the moth 005 / thickness and moth potassium (U parts by weight), the pupa was subjected to a dyeing treatment with a moth ', followed by 5Q. ㈢ 3% in a meal solution to obtain a stretched film. After the extension treatment, the membrane was immersed in a 5 // aqueous solution of pentaponic acid for 2 minutes, and then immersed in an aqueous solution of π. Potassium chloride for 1 minute. After washing with water, Ah, the polarizing film of the present invention is obtained by drying in the air. The boric acid content of the polarizing film is 2 5% by weight, and the gas ion content is 5,000 ppm. 里 〇 'On both sides of the obtained polarizing film, poly After a TAC film (T8uz, made by Fuji Photo Soft) was laminated with an ethylene-based adhesive, it was dried for 70 minutes at 70 ° C to obtain a polarizing plate. This polarizing plate is a colorless one of the ^ phase a * Ul and the hue b * = CK49 in the parallel polarized light. Comparative Example 1 Polyvinyl alcohol (75 μm in thickness) (VF-XS manufactured by Claret Co., Ltd. (Transliteration)) was used. After swelling in water at 30 ° C for 5 minutes, the polyethylene 4 film was dipped in a 35C dyeing solution (100 parts by weight of water, containing 0 μ parts by weight of iodine and 0.1 parts by weight of potassium iodide). For 5 minutes, dysprosium was dyed with iodine, and then stretched 47 times in a 2% boric acid aqueous solution at 50 ° C to obtain an extended film. After the stretching treatment, the stretched film was washed in water of Nachi for 2 minutes, and then dried in air at 40 ° C to obtain a comparative polarizing film. The boric acid content of this polarizing film is 6.5% by weight, and the gas ion content is 30 ppm. 5 Lile 316317 16 * 200521470 On both sides of the polarized film with side spreading, the top layer of TAC film (T80UZ made by Fuji Photo Soft) was applied with polyvinyl alcohol adhesive, and then 60%. 〇Dried for 5 minutes to obtain a polarizing plate. This polarizer is a colorless one with hue a * =-0.87 and hue b * = 0.68 in parallel polarized light. As in the case where the polarizing plates of the present invention and the comparative polarizing plates obtained in Examples 1 to 4 and Comparative Examples are used as ordinary liquid crystal display devices, they are bonded to a glass substrate and a liquid crystal cell (LCD). The test was performed under high temperature conditions (85 C) and high temperature and humidity conditions (60 ° CX 90% RH). The results are shown in Table 1. Table 1 Performance test Results of 85 ° Cx 1000h ~ 60 ° Cx 90% RHTT 〇00h adhered to the LCD Polarization change color change (△ (a * .b *)) Polarization change color change (△ ( a * .b *)) Example 1 +0.3 1.9 -11.9 0.8 Example without display problem 2 +0.5 2.1 -12.4 0.9 Example without user showing problem 3 +0.3 1.8 -15.7 2.8 Example without display problem 4 +03 2.0 -14.4 2.2 No display problem Comparative Example 1 +1.8 10.4 -26.5 4.1 The display is faint and cannot be seen Table 1 shows high temperature conditions (85. 0) and high temperature and humidity conditions (6 (TCx 90%)) Next, the "polarity change", "color change (△ a * .b *)", and "results fitted to the LCD" when the test was performed after the looo hour was separately performed. Among them, the so-called "polarization change" is Refers to the difference between the polarization before and after the test, + means that the polarization after the test is higher than that before the test, "" means that the polarization after the test is less than that before the test. In addition, "color change (△ a * .b *) ”Coefficient formula + △”, Δί3 * Coefficient 316317 -200521470 Don't refer to the change of hue a * in the parallel polarized light before and after the test Amount, change in hue b *. That is, △ (a * .b *) means that the hue of the polarizing plate is doubled before and after the test. Therefore, "the result of fitting to the LCD" means evaluating each test visually. The results of the liquid crystal display state shown in Table 1. As shown in Table 1, the polarization degree of the polarizing plate of the present invention under high-temperature conditions (85. 0 and high-temperature and high-humidity conditions (6Gt: X 9G%)) after long time (_Gh) standing The change is less than that of the polarizing plate shown in Comparative Example 丨, and in addition, compared to the value of the polarizing plate shown in Comparative Example 丨, the value of Erming :: plate color change uw)) is smaller. This shows the polarized light of the present invention ^ Almost no discoloration was caused, that is, the colorless hue was maintained after the test. In addition, the liquid crystal display state of the present invention did not cause any problems. 316317 18